All diseases

OMIM ID
611719
OMIM term:
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 5; COXPD5
Alternative terms:

(∗) Location:
3q23  
(†) Associated OMIM genes:
MRPS22  
(‡) Associated MGI genes:

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Choose a gene on the left to see models here.
* quick link - http://q.sanger.ac.uk/1lyj305e